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"Donohara" dental amalgam capsules (unsterilized) - Taiwan Registration c22a2a6ea082837bed06494aaec60ebb

Access comprehensive regulatory information for "Donohara" dental amalgam capsules (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c22a2a6ea082837bed06494aaec60ebb and manufactured by INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD.. The authorized representative in Taiwan is INOHARA DENTAL INSTRUMENT EQUIPMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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c22a2a6ea082837bed06494aaec60ebb
Registration Details
Taiwan FDA Registration: c22a2a6ea082837bed06494aaec60ebb
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Device Details

"Donohara" dental amalgam capsules (unsterilized)
TW: โ€œไธผๅŽŸโ€็‰™็ง‘็”จๆฑž้ฝŠ่† ๅ›Š(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

c22a2a6ea082837bed06494aaec60ebb

Company Information

Taiwan, Province of China

Product Details

It is limited to the first level identification scope of dental amalgam capsules (F.3110) in the Administrative Measures for Medical Devices.

F Dentistry

F.3110 ็‰™็ง‘็”จๆฑž้ฝŠ่† ๅ›Š

Domestic

Dates and Status

Mar 04, 2010

Mar 04, 2020

Aug 05, 2022

Cancellation Information

Logged out

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